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Selective and universal primers for trematode barcoding in freshwater snails.
J Routtu1, D Grunberg, R Izhar
1Department of Zoology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 6997801, Israel.
Parasitology Research
|May 1, 2014
Summary
Developing a trematode barcoding system using 18S rDNA primers improves species identification in mixed samples. This rapid molecular tool aids in diagnosing medically and environmentally important trematode infections in freshwater snails.
Area of Science:
- Parasitology
- Molecular Biology
- Ecology
Background:
- Trematodes are significant pathogens with medical, veterinary, and environmental importance.
- Isolating trematodes from intermediate hosts and identifying early life stages morphologically is challenging.
Purpose of the Study:
- To develop a species barcoding system for trematodes using selective PCR amplification.
- To create a diagnostic tool for rapid and accurate trematode identification in mixed samples.
Main Methods:
- Development of specific oligonucleotide primers targeting the 18S ribosomal DNA (rDNA) gene.
- Application of PCR amplification for selective detection of trematodes in freshwater snail hosts.
- Utilizing high polymorphism between conserved areas for species classification.
Main Results:
- A universal primer set was developed for trematodes infecting various freshwater snail species in Israel.
- The trematode barcoding system provides rapid identification based on an 800 bp sequence.
- Accurate species classification is achieved due to significant genetic polymorphism.
Conclusions:
- Trematode barcoding offers a fast and accurate alternative to traditional morphological identification.
- This molecular tool is valuable for diagnosing trematode infections in ecological and public health contexts.
- The developed system facilitates the study of trematode diversity and transmission dynamics.

